Canonical Allele Identifier: PA916046411
Gene: MROH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 208941
ClinVar RCV Id: RCV000201373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354436.1:p.Arg651Gln
CA279228
NM_001367507.1:c.1952G>A